Canonical Allele Identifier: PA1139698036
Gene: TNNT2 HGNC NCBI

Linked Data

ClinVar Variation Id: 927049
ClinVar RCV Id: RCV001190057 RCV002375105 RCV002484039 RCV003449619 RCV003449618 RCV003449620
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263274.1:p.Glu143Gln
CA344205938
NM_001276345.2:c.427G>C